EP0202635A2 - Procédé de préparation d'objets façonnés à base de résines de chlorure de vinyle ayant des propriétés de surface améliorées - Google Patents

Procédé de préparation d'objets façonnés à base de résines de chlorure de vinyle ayant des propriétés de surface améliorées Download PDF

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Publication number
EP0202635A2
EP0202635A2 EP86106752A EP86106752A EP0202635A2 EP 0202635 A2 EP0202635 A2 EP 0202635A2 EP 86106752 A EP86106752 A EP 86106752A EP 86106752 A EP86106752 A EP 86106752A EP 0202635 A2 EP0202635 A2 EP 0202635A2
Authority
EP
European Patent Office
Prior art keywords
vinyl chloride
based resin
resin composition
epoxy compound
filler
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP86106752A
Other languages
German (de)
English (en)
Other versions
EP0202635A3 (fr
Inventor
Susumu Shin-Etsu Kagaku Kogyo Ueno
Kouiti Shin-Etsu Kagaku Kogyo Kuroda
Shigehiro Hoshida
Kenji Fushimi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Publication of EP0202635A2 publication Critical patent/EP0202635A2/fr
Publication of EP0202635A3 publication Critical patent/EP0202635A3/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
    • B29C59/005—Surface shaping of articles, e.g. embossing; Apparatus therefor characterised by the choice of material
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
    • B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2027/00—Use of polyvinylhalogenides or derivatives thereof as moulding material
    • B29K2027/06—PVC, i.e. polyvinylchloride

Definitions

  • the present invention relates to a method for the preparation of a shaped article of a vinyl chloride-based resin composition having improved surface properties. More particularly, the invention relates to a method for the preparation of a shaped article of a vinyl chloride-based resin composition having improved surface properties in respect of the insusceptibility to surface stain, weatherability, heat resistance, resistance against chemicals and oils, insusceptibility to blocking, decreased bleeding of plasticizers and others.
  • vinyl chloride-based resins belong to one of the most important classes of general-purpose synthetic plastics by virtue of the versatility in respect of the rigidity of the shaped articles thereof ranging from rigid articles without formulation of a plasticizer to flexible articles prepared by compounding the resin with a substantial amount of a plasticizer.
  • vinyl chloride-based resins are compounded with various kinds of other additives or compounding agents such as stabilizers, lubricants, antioxidants, chelating agents, anti-fogging agents, ultraviolet absorbers, fillers and so on depending on the intended application of the resin composition including films, sheets, artificial leathers, tubes, hoses, packings, covering materials and the like used in medical implements, wrapping materials of foods, insulation of electric wires, building materials and the like.
  • the ionizing radiations usually have high energy so that the effect thereof is sometimes not limited to the very surface of the articles but the radiation penetrates more or less to the depth of the article to cause undesired alterations in the properties of the article due to, for example, formation of intermolecular crosslinks.
  • the surface of the article is sometimes not free from the problem of disadvantageous coloration.
  • the chemical means in the prior art are also not free from the problems in respect of the corrosiveness of the treatment agent, poor adhesion of the agent to affect the durability of the effect by the treatment and so on.
  • a considerably effective method has recently been reported to improve the surface properties of a shaped article of a vinyl chloride-based resin composition that the surface of the shaped article is subjected to a treatment of exposure to an atmosphere of low temperature plasma so as to prevent bleeding of the plasticizer contained therein on the surface.
  • the method of low temperature plasma treatment is indeed effective at least for a length of time immediately following the plasma treatment but the durability of the effect is far from satisfactory since the effect gradually disappears in the lapse of time when the treated article is used prolongedly, especially, in an outdoor condition so that it has been eagerly desired to develop a novel and effective method in the above mentioned object without the problems and disadvantages in the prior art methods.
  • the method of the present invention established as a result of the extensive investigations undertaken in the above mentioned object comprises:
  • the most unique feature of the inventive method is in the compounding of the vinyl chloride-based resin com- . position before shaping with a specific additive which is a filler having been surface-treated with an epoxy compound followed by shaping an article which is then subjected to a low temperature plasma treatment.
  • the shaped article prepared in accordance with the above described method is imparted with markedly improved surface properties including the greatly decreased bleeding of the plasticizer and insusceptibility of the surface to contamination or stain.
  • the advantageous effect obtained in the above described inventive method is quite durable so that the shaped article prepared according to the inventive method can be used prolongedly even under an adverse condition of outdoor exposure without losing the effect obtained by the low temperature plasma treatment.
  • the principal component in the resin composition of which the shaped article is prepared according to the inventive method is of course a vinyl chloride-based resin which is not particularly limited to homopolymeric polyvinyl chloride resins but can be a copolymeric resin obtained by the copolymerization of a monomer mixture composed of vinyl chloride in an amount of, for example, 50 % by weight or more combined with one or more of comonomers copolymerizable with vinyl chloride.
  • the comonomers to be copolymerized with vinyl chloride include vinyl esters, e.g. vinyl acetate, vinyl ethers, acrylic and methacrylic acids and esters thereof, maleic and fumaric acids and esters thereof, maleic anhydride, aromatic vinyl compound, e.g.
  • styrene vinylidene halides, e.g. vinylidene chloride, unsaturated nitriles, e.g. acrylonitrile and methacrylonitrile, olefins, e.g. ethylene and propylene, and the like.
  • vinylidene halides e.g. vinylidene chloride
  • unsaturated nitriles e.g. acrylonitrile and methacrylonitrile
  • olefins e.g. ethylene and propylene, and the like.
  • the specific additive as the component (B) essentially compounded with the above mentioned vinyl chloride-based resin is a filler surface-treated with an epoxy compound.
  • the filler is not particularly limited to a particular kind but may be any of particulate or fibrous materials used conventionally in vinyl chloride-based resin compositions although calcium carbonate and titanium dioxide are preferable.
  • the epoxy compound for the surface treatment of the filler is also not particularly limitative provided that the compound has at least one epoxy group in a molecule.
  • Particularly suitable ones are exemplified by 3-glycidyloxypropyl trimethoxy silane and a hydrolysis-condensation product thereof, 3-glycidyloxypropyl triethoxy silane and a hydrolysis-condensation product thereof, phenyl glycidyl ether, ethyleneglycol diglycidyl ether, vinyl cyclohexene diepoxide, N,N-diglycidylamine, divinylbenzene diepoxide, resorcinol diglycidyl ether, polyepichlorohydrin, triglycidyl cyanurate, 1,3-bis(N,N-diglycidylaminomethyl) cyclohexane, N,N,N'N'-tetraglycidyl 1,3-xylenediamine and the like, of which the first mentioned epoxy-containing organosilicon compounds or hydrolysis-condensation products thereof give quite satisfactory results.
  • the surface treatment of the filler with the epoxy compound can be carried out in any convenient procedure including wet blending and dry blending.
  • a filler surface-treated with the epoxy compound can be prepared by a simple procedure of merely blending the filler and the epoxy compound in a suitable mixing machine such as a Henschel mixer and the like.
  • the overall amount of the filler incorporated into the resin composition should not exceed 100 parts by weight or, preferably, 50 parts by weight per 100 parts by weight of the vinyl chloride-based resin as the component (A).
  • An excessively large amount of a filler is undesirable due to the possible adverse influences on the mechanical and other properties of the shaped articles of the resin composition.
  • the amount of the epoxy compound incorporated into the resin composition as carried by the filler should be in the range from 0.05 to 30 parts by weight or, preferably, from 0.5 to 10 parts by weight per 100 parts by weight of the vinyl chloride-based resin. When the amount thereof is too small, the desired advantageous effect of the inventive method cannot be obtained as a matter of course. An amount of the epoxy compound in excess of the above mentioned upper limit is not detrimental in respect of the properties of the resin composition or the shaped articles thereof though with economical disadvantages. It is not essential that the surface treatment of the filler with the epoxy compound is uniform over the whole amount of the filler but a portion of the filler is surface-treated with the epoxy compound and the thus surface-treated filler is combined with a supplementary portion of the untreated filler.
  • the vinyl chloride-based resin composition composed of a vinyl chloride-based resin and the surface-treated filler in the above mentioned specific proportion can of course be further admixed according to need with various kinds of known additives and compounding agents conventionally used in vinyl chloride-based resin compositions for shaping articles.
  • the plasticizers to impart flexibility to the shaped articles are exemplified by phthalate esters, e.g. dioctyl phthalate, dibutyl phthalate and butyl benzyl phthalate, esters of aliphatic dibasic acids, e.g.
  • dioctyl adipate and dibutyl sebacate esters of pentaerithritol, esters of glycols, e.g. diethyleneglycol dibenzoate, esters of monobasic carboxylic acids, e.g. methyl acetylricinolate, phosphate esters, e.g. tricresyl phosphate and triphenyl phosphate, epoxidized oils, e.g. epoxidized soybean oil and epoxidized linseed oil, citric acid esters, e.g. acetyl tributyl citrate and acetyl trioctyl citrate, polyester-type compounds, e.g. trialkyl trimellitates, tetra-n-octyl pyro- mellitate and polypropylene adipate, and so on.
  • polyester-type compounds e.g. trialkyl trimellitates, tetra-
  • the optional additives include stabilizers used to impart heat resistance and stability to the shaped articles exemplified by metal salts of carboxylic acids, e.g. calcium stearate, zinc stearate, lead stearate, barium stearate and cadmium stearate, lead compounds, e.g. tribasic lead sulfate and dibasic lead phosphite, organic tin compounds, e.g.
  • carboxylic acids e.g. calcium stearate, zinc stearate, lead stearate, barium stearate and cadmium stearate
  • lead compounds e.g. tribasic lead sulfate and dibasic lead phosphite
  • organic tin compounds e.g.
  • fatty acid amides e.g. ethylene bisste- aroamide, higher fatty acids and esters thereof, polyethyl- .ene waxes and the like
  • fillers e.g. ethylene bisste- aroamide, higher fatty acids and esters thereof, polyethyl- .ene waxes and the like, fillers, antioxidants, ultraviolet absorbers, antistatic agents, anti
  • the resin composition is admixed with a rubbery polymer to improve the physical properties of the shaped articles.
  • Suitable rubbery polymers having compatibility with the vinyl chloride-based resin include copolymers of ethylene and vinyl acetate, copolymers of acrylonitrile and butadiene, copolymers of styrene and acrylonitrile, copolymers of methyl methacrylate, styrene and butadiene, urethane elastomers, copolymers of acrylonitrile, styrene and butadiene, polyamide resins, polymers of caprolactam, epoxy-modified polybutadiene resins and the like.
  • the amount of these rubbery polymers in the resin composition should not be excessively large or should not exceed 50 parts by weight per 100 parts by weight of the vinyl chloride-based resin in order to retain the excellent properties inherent in the vinyl chloride-based resins.
  • step (a) of the inventive method in which the vinyl chloride-based resin composition is prepared according to the above described manner is followed by the step (b) for shaping the resin composition into a shaped article.
  • the method for shaping the resin composition is not particularly limitative and any of the conventional methods known in the art is applicable depending on the nature of the resin composition and the type of the desired shaped articles including extrusion molding, injection molding, calendering, inflation, compression molding and so on without particular limitations.
  • the shaped article of the resin composition obtained in the step (b) of the inventive method is then subjected to a low temperature plasma treatment in the step (c) by exposing the article to an atmosphere of low temperature plasma of an inorganic gas under a reduced pressure in the range from 0.001 to 10 Torr or, preferably, from . 0.01 to 1 Torr.
  • the shaped article is placed in a vacuumizable plasma chamber in which electrodes are installed and, while the pressure inside the chamber is kept under the above mentioned reduced pressure by the balance of the continuous introduction of an inorganic gas into and continuous evacuation of the chamber, an electric power of 10 watts to 100 kilowatts at a frequency of, for example, 10 kHz to 100 MHz is impressed between the electrodes to cause glow discharge so that low temperature plasma of the inorganic gas'is generated inside the chamber to which the shaped article of the resin composition is exposed. It is not essential that the frequency of the electric power is within the above mentioned high frequency range but can be direct current or in the range of low frequencies and microwaves.
  • the electrodes are installed preferably inside the plasma chamber as is mentioned above, the electrodes may be installed outside the plasma chamber.
  • a single high-frequency work coil surrounding the plasma chamber also may serve as an electrode for the generation of low temperature plasma.
  • These electrodes are connected to a high frequency generator either by capacitive coupling or inductive coupling. At any rate, it is essential that care should be taken not to cause any adverse thermal denaturation on the surface of the shaped article under the treatment by the excessive heat of electric discharge.
  • the form of the electrodes which should be installed preferably inside the plasma chamber, is not particularly limitative including plate-like, ring-like, rod-like, cylindrical and any other forms.
  • the grounded electrode and the power electrode may be either of the same form or of different forms from each other. It is a convenient design of the plasma chamber that the chamber walls are made of a metal to serve as the grounded electrode surrounding the power electrode installed therein.
  • the material of the electrodes may be copper, iron, aluminum and the like. It is preferable that the surface of, at least, the power electrode is provided with an insulating coating of a heat-resistant material such as glass, porcelain enamel, ceramic and the like having a breakdown voltage of at least 10,000 V to ensure stability of the electric discharge.
  • Suitable inorganic gases for forming the atmosphere of low temperture plasma are exemplified by helium, argon, nitrogen, nitrous oxide, nitrogen dioxide, oxygen, air, carbon monoxide, carbon dioxide, hydrogen, chlorine, hydrogen chloride, sulfur dioxide, hydrogen sulfide and the like. These inorganic gases can be used either singly or as a mixture of two kinds or more according to need.
  • the pressure of the plasma-supporting inorganic gas inside the plasma chamber should be in the range from 0.001 to 10 Torr as is mentioned above or, preferably, from 0.01 to 1 Torr in order to ensure stability of the plasma generation.
  • the surface layer of the article is converted to a barrier layer having flexibility and an adequately controlled degree of crosslinking so as to effectively prevent bleeding of the plasticizer and other additives compounded in the resin composition.
  • the barrier layer thus formed is not detrimental against the heat-sealability of the shaped articles as in the high-frequency welding.
  • the barrier layer has excellent durability so that the advantageous effects of the inventive method can be fully retained even after prolonged outdoor exposure of the shaped article.
  • the advantages obtained by the inventive method are not only the above mentioned reduced or prevented bleeding of the plasticizer and other additives on the surface but the shaped articles prepared according to the inventive method are excellent in respect of other surface properties such as hydrophilicity, insusceptibility to stain, resistance against oils and chemicals and so on.
  • each of the resin sheets either before or after the low temperature plasma treatment was subjected to the tests of the plasticizer, i.e. dioctyl phthalate, extraction and contamination with a contaminant blend.
  • the testing procedures were as given below. The tests were undertaken with the resin sheets either before or after accelerated aging in a Weather-o-meter for 100 hours or 500 hours.
  • a piece of the resin sheet was placed on the bottom of a cylindrical vessel having a capacity of 100 ml in such a manner that a surface area of 26 cm 2 of the resin sheet was exposed and contacted with 50 ml of n-hexane as a solvent introduced into the vessel.
  • the vessel was shaken for 2 hours in a thermostat at 37 o C and the solvent was analyzed by gas chromatography to determine the concentration of dioctyl phthalate therein extracted out of the resin sheet.
  • a contaminant blend was prepared by mixing together 380 g of Knuma earth, 170 g of carbon black, 170 g of portland cement, 170 g of finely divided silica flour, 85 g of bentonite, 85 g of kaolin, 5 g of iron oxide (Fe 3 0 4 ) powder and 87 g of turbine oil and the blend was introduced into a polyethylene-made wide-mouth bottle of 5 liter capacity and thoroughly shaken. Thereafter, a 3 cm by 3 cm wide piece of the resin sheet was put into the bottle and thoroughly shaken together with the contaminant blend. The bottle was kept at 80 o C in a Geer's oven for 15 minutes and taken out of the oven to be shaken again followed by second heating for another 15 minutes.
  • a resin composition was prepared by compounding 100 parts of a homopolymeric polyvinyl chloride resin (TK-1300, a product by Shin-Etsu Chemical Co.), 50 parts of dioctyl phthalate, 2.5 parts of a stabilizer based on barium and zinc compounds, 5 parts of an epoxidized soybean oil and 25 parts of the above prepared surface-treated filler and the resin composition was milled on a roller mill at 160 °C for 10 minutes followed by compression molding at a temperature of 170 O C into a sheet having a thickness of 0.5 mm.
  • This sheet as prepared is referred to as the Sheet A hereinbelow.
  • the Sheet A was subjected to a low temperature plasma treatment for 10 seconds in a plasma chamber under a continuous flow of carbon monoxide gas to keep a pressure at 0.1 Torr while low temperature plasma was generated inside the chamber by the impression of a high frequency electric power of 20 kilowatts at a frequency of 110 kHz.
  • the density of the electric power on the surface of the power electrode was 3.3 kilowatts/cm 2 .
  • the thus plasma-treated sheet is referred to as the Sheet B hereinbelow.
  • the formulation of the resin composition and the procedure for the preparation of a resin sheet of the resin composition were the same as in Example 1 except that the calcium carbonate filler surface-treated with the epoxy compound in advance was replaced with 25 parts of the untreated calcium carbonate filler and 5 parts of 3-glycidyloxypropyl trimethoxy silane separately added to the mixer.
  • the resin sheet thus prepared is referred to as the Sheet C hereinbelow.
  • the Sheet C was subjected to the low temperature plasma treatment in the same manner under the same conditions as in Example 1.
  • the thus plasma-treated sheet is referred to as the Sheet D hereinbelow.
  • Each of the Sheets C and D was subjected to the tests in the same manner as in Example 1 to give the results shown in Table 1.
  • the formulation of the resin composition and the procedure for the preparation of a sheet of the resin composition were the same as in Example 1 except that the clacium carbonate filler surface-treated with the epoxy compound was replaced with the same amount of the untreated calcium carbonate filler.
  • the resin sheet thus prepared is referred to as the Sheet E hereinbelow.
  • the Sheet E was subjected to a low temperature plasma treatment in the same manner and under the same conditions as in Example 1.
  • the thus plasma-treated resin sheet is referred to as the Sheet F hereinbelow.
  • Each of the Sheets E and F was subjected to the tests in the same manner as in Example 1 to give the results shown in Table 1.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP86106752A 1985-05-21 1986-05-16 Procédé de préparation d'objets façonnés à base de résines de chlorure de vinyle ayant des propriétés de surface améliorées Withdrawn EP0202635A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP60109003A JPS61266438A (ja) 1985-05-21 1985-05-21 表面特性の改質された塩化ビニル系樹脂成形品の製造方法
JP109003/85 1985-05-21

Publications (2)

Publication Number Publication Date
EP0202635A2 true EP0202635A2 (fr) 1986-11-26
EP0202635A3 EP0202635A3 (fr) 1988-06-22

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EP86106752A Withdrawn EP0202635A3 (fr) 1985-05-21 1986-05-16 Procédé de préparation d'objets façonnés à base de résines de chlorure de vinyle ayant des propriétés de surface améliorées

Country Status (3)

Country Link
US (1) US4722816A (fr)
EP (1) EP0202635A3 (fr)
JP (1) JPS61266438A (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102558714A (zh) * 2011-06-24 2012-07-11 云南鑫乾矿业有限公司 一种聚氯乙烯／改性纳米蒙脱石复合材料及其制备方法
CN105482144A (zh) * 2015-12-15 2016-04-13 广东萨提亚新型建材科技有限公司 一种抗菌抗霉石塑板材及其制备方法
EP3693407A1 (fr) * 2019-02-11 2020-08-12 Omya International AG Produit de matériau de remplissage traité en surface assurant une meilleure stabilité aux uv aux articles polymères

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US4820750A (en) * 1988-02-11 1989-04-11 The B.F. Goodrich Company Pigmented vinyl chloride polymer or blend thereof having improved mechanical properties
DE3811449A1 (de) * 1988-04-06 1989-10-19 Bayer Ag Verfahren zur verminderung der fogentwicklung durch weichmacher in kunststoffen
US5236649A (en) * 1988-12-23 1993-08-17 The Dow Chemical Extrudable thermoplastic particulates
CN1167733C (zh) 1999-06-16 2004-09-22 花王株式会社 表面改性剂
DE10164408A1 (de) * 2001-12-28 2003-07-17 Degussa Flüssigkeits- oder dampfführendes System mit einer Fügezone aus einem coextrudierten Mehrschichtverbund
US8337734B2 (en) 2010-09-10 2012-12-25 Carefusion 303, Inc. Non-stick medical tubing
US8916067B2 (en) 2011-10-19 2014-12-23 The Aerospace Corporation Carbonaceous nano-scaled materials having highly functionalized surface
WO2016004325A1 (fr) * 2014-07-02 2016-01-07 Imerys Pigments, Inc. Mélanges de carbonate revêtu d'acide gras avec du carbonate non traité destiné à être utilisé dans le traitement en fusion de polymères chargés de carbonate
CN113861477B (zh) * 2021-09-30 2022-06-10 无锡市金华屹圆科技有限公司 一种冰箱用pvc管及其表面处理工艺

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GB2025982A (en) * 1978-06-26 1980-01-30 Agency Ind Science Techn Method for preventing plasticizer bleeding on polyvinyl chloride shaped articles
EP0106363A2 (fr) * 1982-10-19 1984-04-25 Toray Silicone Co., Ltd. Compositions de polyorganosiloxane vulcanisables à température ambiante, résistantes à l'eau, et procédé pour les préparer

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GB1095700A (en) * 1965-12-20 1967-12-20 Ici Ltd Reinforcing thermoplastics
GB2025982A (en) * 1978-06-26 1980-01-30 Agency Ind Science Techn Method for preventing plasticizer bleeding on polyvinyl chloride shaped articles
EP0106363A2 (fr) * 1982-10-19 1984-04-25 Toray Silicone Co., Ltd. Compositions de polyorganosiloxane vulcanisables à température ambiante, résistantes à l'eau, et procédé pour les préparer

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102558714A (zh) * 2011-06-24 2012-07-11 云南鑫乾矿业有限公司 一种聚氯乙烯／改性纳米蒙脱石复合材料及其制备方法
CN102558714B (zh) * 2011-06-24 2013-09-18 云南鑫乾矿业有限公司 一种聚氯乙烯／改性纳米蒙脱石复合材料及其制备方法
CN105482144A (zh) * 2015-12-15 2016-04-13 广东萨提亚新型建材科技有限公司 一种抗菌抗霉石塑板材及其制备方法
CN105482144B (zh) * 2015-12-15 2019-03-19 广东萨提亚新型建材科技有限公司 一种抗菌抗霉石塑板材及其制备方法
EP3693407A1 (fr) * 2019-02-11 2020-08-12 Omya International AG Produit de matériau de remplissage traité en surface assurant une meilleure stabilité aux uv aux articles polymères
WO2020165138A1 (fr) * 2019-02-11 2020-08-20 Omya International Ag Produit à base de matériau de charge traité en surface assurant une stabilité aux uv améliorée pour des articles polymères

Also Published As

Publication number Publication date
US4722816A (en) 1988-02-02
JPS61266438A (ja) 1986-11-26
JPH0447698B2 (fr) 1992-08-04
EP0202635A3 (fr) 1988-06-22

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